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    An electron diffraction study of the structure of the molecules of tris (dimethylamino) phosphine P[N(CH3)2]3 and tris(ethyleneimino) phosphine P[N(CH2)2]3
    Journal of Structural Chemistry (1970)
    Л. В. ВилковL. S. KhaikinВ. В. Евдокимов
    Solid-state physics
    Citations (3)
    High basicity of phosphorus–proton affinity of tris-(tetramethylguanidinyl)phosphine and tris-(hexamethyltriaminophosphazenyl)phosphine by DFT calculations
    Chemical Communications (2006)
    Borislav KovačevićZvonimir B. Maksić
    It is shown by approximate but reliable DFT calculations that the title compounds represent very strong superbases in gas phase and MeCN. In particular, tris-(hexamethyltriaminophosphazenyl)phosphine has a proton affinity, PA, of 295.5 kcal mol−1 and records a pKa(MeCN) of 50 ± 1 units.
    Proton affinity
    Citations (60)
    Synthesis of the tertiaryphosphine derivatives of iron carbonyl phosphines: preparation of tetracarbonyl[tris(2-furyl)phosphine]iron(0), pentacarbonylbis[μ-bis(2-furyl)phosphido]-[tris(2-furyl)phosphine]diiron(0), tetracarbonyl[tris(2-benzofuryl) phosphine]iron(0) and pentacarbonylbis[μ-bis(2-benzofuryl) phosphido]-[tris(2-benzofuryl) phosphine]diiron-(0)
    Journal of Organometallic Chemistry (1995)
    Christiane Santelli‐RouvierChristine CoinLoı̈c ToupetMaurice Santelli
    Sodium borohydride
    Citations (16)
    A new tris(ferrocenylamine) ditertiary phosphine: Synthesis and co-ordination studies
    Journal of Organometallic Chemistry (2010)
    M.R.J. ElsegoodA.J. LakeRoger J. MortimerMartin B. SmithGeorge W. Weaver
    Citations (7)
    Diiron propane-1,2-dithiolate complexes with monosubstituted tris(3-chlorophenyl)phosphine or tris(4-trifluoromethylphenyl)phosphine: synthesis, characterization, crystal structures, and electrochemistry
    Inorganic and Nano-Metal Chemistry (2020)
    Yan LinLinghui WangJun YangXu‐Feng LiuYu‐Long Li
    (2020). Diiron propane-1,2-dithiolate complexes with monosubstituted tris(3-chlorophenyl)phosphine or tris(4-trifluoromethylphenyl)phosphine: synthesis, characterization, crystal structures, and electrochemistry. Inorganic and Nano-Metal Chemistry: Vol. 50, No. 11, pp. 1137-1143.
    Propane
    Citations (2)
    Reactions of polyfluoroalkanethioamides with tris(diethylamino)phosphine
    Russian Journal of Organic Chemistry (2013)
    Nadiia V. PikunSergiy S. МykhaylychenkoЭдуард Б. РусановYu. G. Shermolovich
    Citations (2)
    Optically active phosphine oxides. 8
    Tetrahedron (1989)
    K.M. PietrusiewiczWitold WiśniewskiMaria Zabłocka
    Phosphine oxide
    Citations (33)
    Structural and electronic properties of tris(4-trifluoromethyltetrafluorophenyl)phosphine
    Journal of Fluorine Chemistry (2015)
    Graham C. Saunders
    Ligand cone angle
    Citations (1)
    Tris(n-propyl)phosphine and Tris(isopropyl)phosphine
    Acta Crystallographica Section C Crystal Structure Communications (1996)
    J. BruckmannCarsten Krüger
    Single crystals of the low-melting title compound, tris(n-propyl)phosphine, C9H21P, (1), and its isomer, tris(isopropyl)phosphine, (2), were grown in situ in capillaries. The crystal and molecular structures of both compounds were determined at 102 K. Compound (1) has an approximate mirror plane and C—P—C angles between 99.8 (1) and 102.3 (1)°, whereas compound (2) displays no molecular symmetry and C—P—C angles ranging from 102.0 (1) to 104.7 (1)°.
    Isopropyl
    Citations (8)